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6-Chloro-7-Methyl-[1,2,4]Triazolo[4,3-B]Pyridazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58826-39-4

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58826-39-4 Usage

Structure

Heterocyclic compound containing a triazole ring fused with a pyridazine ring

Primary Use

Pharmaceutical intermediate for synthesizing various drugs and active pharmaceutical ingredients

Biological Activities

Antimicrobial: Studied for antimicrobial properties
Antiviral: Investigated for potential antiviral activity
Antitumor: Research conducted on its potential as an antitumor agent

Stability

Stable under normal temperatures and pressures

Application

Valuable compound for research and development in the pharmaceutical industry

Check Digit Verification of cas no

The CAS Registry Mumber 58826-39-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,8,2 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 58826-39:
(7*5)+(6*8)+(5*8)+(4*2)+(3*6)+(2*3)+(1*9)=164
164 % 10 = 4
So 58826-39-4 is a valid CAS Registry Number.

58826-39-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-7-methyl-[1,2,4]triazolo[4,3-b]pyridazine

1.2 Other means of identification

Product number -
Other names 6-chloro-7-methyl[1,2,4]triazolo[4,3-b]pyridazine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:58826-39-4 SDS

58826-39-4Downstream Products

58826-39-4Relevant academic research and scientific papers

Nucleophilic substitution and lipophilicity - Structure relations in methylazolopyridazines

Katrusiak, Anna,Ratajczak-Sitarz, Malgorzata,Skierska, Urszula,Zinczenko, Wiktoria

, p. 1372 - 1386 (2007/10/03)

Syntheses of methyl[1,2,4]triazolo- or methyltetrazolopyridazine isomers, their separation and nucleophilic substitution with morpholine, dimethylamine and hydrazine have been described. The lipophilicity of the azolopyridazines has been measured and rela

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